hERG channel agonist NS1643 strongly inhibits invasive astrocytoma cell line SMA-560

Gliomas are highly malignant brain tumours that remain refractory to treatment. Treatment is typically surgical intervention followed by concomitant temozolomide and radiotherapy; however patient prognosis remains poor. Voltage gated ion channels have emerged as novel targets in cancer therapy and inhibition of a potassium selective subtype (hERG, Kv11.1) has demonstrated antitumour activity. Unfortunately blockade of hERG has been limited by cardiotoxicity, however hERG channel agonists have produced similar chemotherapeutic benefit without significant side effects. In this study, electrophysiological recordings suggest the presence of hERG channels in the anaplastic astrocytoma cell line SMA-560, and treatment with the hERG channel agonist NS1643, resulted in a significant reduction in the proliferation of SMA-560 cells. In addition, NS1643 treatment also resulted in a reduction of the secretion of matrix metalloproteinase-9 and SMA-560 cell migration. When combined with temozolomide, an additive impact was observed, suggesting that NS1643 may be a suitable adjuvant to temozolomide and limit the invasiveness of glioma.

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Journal
PLoS ONE
Published
2024-09-06
DOI
https://doi.org/10.1371/journal.pone.0309438
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1
Primary Topic
Neuroscience and Neural Engineering
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article
Field-Weighted Citation Impact
0.27
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article

hERG channel agonist NS1643 strongly inhibits invasive astrocytoma cell line SMA-560

Rodney B. Luwor, Kieran W Benn, Stanley S Stylii, Christopher R French et al.
1 citations
PLoS ONE
Neuroscience and Neural Engineering
0.27
article

hERG channel agonist NS1643 strongly inhibits invasive astrocytoma cell line SMA-560

Rodney B. Luwor, Kieran W Benn, Stanley S Stylii, Christopher R French, Harvey K. Chong, Patrick H. Yuan
article en
1 citations

Abstract

Gliomas are highly malignant brain tumours that remain refractory to treatment. Treatment is typically surgical intervention followed by concomitant temozolomide and radiotherapy; however patient prognosis remains poor. Voltage gated ion channels have emerged as novel targets in cancer therapy and inhibition of a potassium selective subtype (hERG, Kv11.1) has demonstrated antitumour activity. Unfortunately blockade of hERG has been limited by cardiotoxicity, however hERG channel agonists have produced similar chemotherapeutic benefit without significant side effects. In this study, electrophysiological recordings suggest the presence of hERG channels in the anaplastic astrocytoma cell line SMA-560, and treatment with the hERG channel agonist NS1643, resulted in a significant reduction in the proliferation of SMA-560 cells. In addition, NS1643 treatment also resulted in a reduction of the secretion of matrix metalloproteinase-9 and SMA-560 cell migration. When combined with temozolomide, an additive impact was observed, suggesting that NS1643 may be a suitable adjuvant to temozolomide and limit the invasiveness of glioma.

PLoS ONEVol. 19(9)
The Royal Melbourne Hospital (AU), The University of Melbourne (AU)
Good health and well-being
Openalex Percentile: Top 45%
Neuroscience and Neural Engineering
0.27
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